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Oxcarbazepine - 49349-785-02 - (Oxcarbazepine)

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Drug Information of Oxcarbazepine

Product NDC: 49349-785
Proprietary Name: Oxcarbazepine
Non Proprietary Name: Oxcarbazepine
Active Ingredient(s): 150    mg/1 & nbsp;   Oxcarbazepine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxcarbazepine

Product NDC: 49349-785
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078069
Marketing Category: ANDA
Start Marketing Date: 20110927

Package Information of Oxcarbazepine

Package NDC: 49349-785-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-785-02)

NDC Information of Oxcarbazepine

NDC Code 49349-785-02
Proprietary Name Oxcarbazepine
Package Description 30 TABLET in 1 BLISTER PACK (49349-785-02)
Product NDC 49349-785
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxcarbazepine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110927
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name OXCARBAZEPINE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Oxcarbazepine


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